Parkinsonism with polyneuropathy

Preferred Label : Parkinsonism with polyneuropathy;

Symbol : PKNPY;

Type : Phenotype, molecular basis known;

Prefixed ID : #619279;

Details

Origin ID

619279;

UMLS CUI

C5543299;

Currated CISMeF NLP mapping
- Parkinsonism with Polyneuropathy [NCIt concept]
- Parkinsonism with polyneuropathy [ORDO Disease]
Genes related to phenotype
- Ubiquinol-cytochrome C reductase core protein I [OMIM gene]
HPO term(s)
- Anxiety [HPO term]
- Autosomal dominant inheritance [HPO term]
- Bradykinesia [HPO term]
- Decreased amplitude of sensory action potentials [HPO term]
- Decreased compound muscle action potential amplitude [HPO term]
- Decreased motor nerve conduction velocity [HPO term]
- Depression [HPO term]
- Diffuse cerebral atrophy [HPO term]
- Late onset [HPO term]
- Middle age onset [HPO term]
- Parkinsonism with favorable response to dopaminergic medication [HPO term]
- Polyneuropathy [HPO term]
- Resting tremor [HPO term]
- Rigidity [HPO term]
ORDO concept(s)
- Parkinsonism with polyneuropathy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Parkinsonism with Polyneuropathy [NCIt concept]

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